Nitrous oxide (N2O) has a global warming potential that is 300 times that of carbon dioxide on a 100-y timescale, and is of major importance for stratospheric ozone depletion. The climate sensitivity of N2O emissions is poorly known, which makes it difficult to project how changing fertilizer use and climate will impact radiative forcing and the ozone layer. Analysis of 6 y of hourly N2O mixing ratios from a very tall tower within the US Corn Belt—one of the most intensive agricultural regions of the world—combined with inverse modeling, shows large interannual variability in N2O emissions (316 Gg N2O-N⋅y−1to 585 Gg N2O-N⋅y−1). This implies that the regional emission factor is highly sensitive to climate. In the warmest year and spring (2012) of the observational period, the emission factor was 7.5%, nearly double that of previous reports. Indirect emissions associated with runoff and leaching dominated the interannual variability of total emissions. Under current trends in climate and anthropogenic N use, we project a strong positive feedback to warmer and wetter conditions and unabated growth of regional N2O emissions that will exceed 600 Gg N2O-N⋅y−1, on average, by 2050. This increasing emission trend in the US Corn Belt may represent a harbinger of intensifying N2O emissions from other agricultural regions. Such feedbacks will pose a major challenge to the Paris Agreement, which requires large N2O emission mitigation efforts to achieve its goals.
Nitrous oxide (N2O) emissions within the US Corn Belt have been previously estimated to be 200–900% larger than predictions from emission inventories, implying that one or more source categories in bottom‐up approaches are underestimated. Here we interpret hourly N2O concentrations measured during 2010 and 2011 at a tall tower using a time‐inverted transport model and a scale factor Bayesian inverse method to simultaneously constrain direct and indirect agricultural emissions. The optimization revealed that both agricultural source categories were underestimated by the Intergovernmental Panel on Climate Change (IPCC) inventory approach. However, the magnitude of the discrepancies differed substantially, ranging from 42 to 58% and from 200 to 525% for direct and indirect components, respectively. Optimized agricultural N2O budgets for the Corn Belt were 319 ± 184 (total), 188 ± 66 (direct), and 131 ± 118 Gg N yr−1 (indirect) in 2010, versus 471 ± 326, 198 ± 80, and 273 ± 246 Gg N yr−1 in 2011. We attribute the interannual differences to varying moisture conditions, with increased precipitation in 2011 amplifying emissions. We found that indirect emissions represented 41–58% of the total agricultural budget, a considerably larger portion than the 25–30% predicted in bottom‐up inventories, further highlighting the need for improved constraints on this source category. These findings further support the hypothesis that indirect emissions are presently underestimated in bottom‐up inventories. Based on our results, we suggest an indirect emission factor for runoff and leaching ranging from 0.014 to 0.035 for the Corn Belt, which represents an upward adjustment of 1.9–4.6 times relative to the IPCC and is in agreement with recent bottom‐up field studies.
Abstract. We quantify methane emissions in China and the contributions from different sectors by inverse analysis of 2019 TROPOMI satellite observations of atmospheric methane. The inversion uses as a prior estimate the latest 2014 national sector-resolved anthropogenic emission inventory reported by the Chinese government to the United Nations Framework Convention on Climate Change (UNFCCC) and thus serves as a direct evaluation of that inventory. Emissions are optimized with a Gaussian mixture model (GMM) at up to 0.25∘×0.3125∘ resolution. The optimization is done analytically assuming log-normally distributed errors on prior emissions. Errors and information content on the optimized estimates are obtained directly from the analytical solution and also through a 36-member inversion ensemble. Our best estimate for total anthropogenic emissions in China is 65.0 (57.7–68.4) Tg a−1, where parentheses indicate the uncertainty range determined by the inversion ensemble. Contributions from individual sectors include 16.6 (15.6–17.6) Tg a−1 for coal, 2.3 (1.8–2.5) for oil, 0.29 (0.23–0.32) for gas, 17.8 (15.1–21.0) for livestock, 9.3 (8.2–9.9) for waste, 11.9 (10.7–12.7) for rice paddies, and 6.7 (5.8–7.1) for other sources. Our estimate is 21% higher than the Chinese inventory reported to the UNFCCC (53.6 Tg a−1), reflecting upward corrections to emissions from oil (+147 %), gas (+61 %), livestock (+37 %), waste (+41 %), and rice paddies (+34 %), but downward correction for coal (−15 %). It is also higher than previous inverse studies (43–62 Tg a−1) that used the much sparser GOSAT satellite observations and were conducted at coarser resolution. We are in particular better able to separate coal and rice emissions. Our higher livestock emissions are attributed largely to northern China where GOSAT has little sensitivity. Our higher waste emissions reflect at least in part a rapid growth in wastewater treatment in China. Underestimate of oil emissions in the UNFCCC report appears to reflect unaccounted-for super-emitting facilities. Gas emissions in China are mostly from distribution, in part because of low emission factors from production and in part because 42 % of the gas is imported. Our estimate of emissions per unit of domestic gas production indicates a low life-cycle loss rate of 1.7 % (1.3 %–1.9 %), which would imply net climate benefits from the current “coal-to-gas” energy transition in China. However, this small loss rate is somewhat misleading considering China's high gas imports, including from Turkmenistan where emission per unit of gas production is very high.
Abstract. We present a user-friendly, cloud-based facility for quantifying methane emissions with 0.25∘ × 0.3125∘ (≈ 25 km × 25 km) resolution by inverse analysis of satellite observations from the TROPOspheric Monitoring Instrument (TROPOMI). The facility is built on an Integrated Methane Inversion optimal estimation workflow (IMI 1.0) and supported for use on the Amazon Web Services (AWS) cloud. It exploits the GEOS-Chem chemical transport model and TROPOMI data already resident on AWS, thus avoiding cumbersome big-data download. Users select a region and period of interest, and the IMI returns an analytical solution for the Bayesian optimal estimate of period-average emissions on the 0.25∘ × 0.3125∘ grid including error statistics, information content, and visualization code for inspection of results. The inversion uses an advanced research-grade algorithm fully documented in the literature. An out-of-the-box inversion with rectilinear grid and default prior emission estimates can be conducted with no significant learning curve. Users can also configure their inversions to infer emissions for irregular regions of interest, swap in their own prior emission inventories, and modify inversion parameters. Inversion ensembles can be generated at minimal additional cost once the Jacobian matrix for the analytical inversion has been constructed. A preview feature allows users to determine the TROPOMI information content for their region and time period of interest before actually performing the inversion. The IMI is heavily documented and is intended to be accessible by researchers and stakeholders with no expertise in inverse modelling or high-performance computing. We demonstrate the IMI's capabilities by applying it to estimate methane emissions from the US oil-producing Permian Basin in May 2018.
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